Literature DB >> 20149413

Use of immunohistochemistry for IgG4 in the distinction of autoimmune pancreatitis from peritumoral pancreatitis.

Deepti Dhall1, Arief A Suriawinata, Laura H Tang, Jinru Shia, David S Klimstra.   

Abstract

The patients with autoimmune pancreatitis usually present with jaundice and a pancreatic head mass, presumed to have pancreatic cancer, and they often undergo pancreatic resection. Elevated serum IgG4 levels (>135 mg/dL) help to distinguish autoimmune pancreatitis from pancreatic cancer. However, when the biopsy from a pancreatic mass shows dense chronic inflammation and fibrosis and the serum IgG4 level is not available, it presents a diagnostic dilemma whether it represents autoimmune pancreatitis or peritumoral pancreatitis. We performed IgG4 immunohistochemistry on 25 cases of autoimmune pancreatitis-lymphoplasmacytic sclerosing pancreatitis, 7 cases of autoimmune pancreatitis with granulocytic epithelial lesions, 8 cases of nonspecific pancreatitis, 15 cases of pancreatitis associated with pancreatic ductal adenocarcinoma, and 5 biopsies of pancreatic adenocarcinoma with variable inflammation. The distribution of IgG4-positive cells was noted in each case. Eighty-four percent (21/25) of autoimmune pancreatitis-LPSP cases showed diffuse and dense staining for IgG4, with more than 50 positive plasma cells per high-power field (range, 50-150 cells/hpf) in the highest density area. Most (5/7) cases of autoimmune pancreatitis-granulocytic epithelial lesions were negative for IgG4. Thirty-nine percent of nonspecific pancreatitis and peritumoral pancreatitis cases stained positive for IgG4, but the distribution was focal and none of the cases showed more than 50 IgG4-positive cells/hpf in the highest density area of IgG4 staining. IgG4-positive cells in peritumoral pancreatitis and nonspecific pancreatitis cases were closely associated with malignant glands and areas of acute inflammation in some cases. Using a cutoff of 50 IgG4-positive cells/hpf, the sensitivity of IgG4 staining for classical autoimmune pancreatitis-LPSP versus other types of pancreatitis was 84%, the specificity was 100%, and the P value was significant (<.0001). Hence, we conclude that diffuse and dense staining (>50 positive cells/hpf) for IgG4 is specifically seen in autoimmune pancreatitis-LPSP, and IgG4 staining along with the histologic features and serum IgG4 levels may be very helpful in diagnosing autoimmune pancreatitis. Copyright 2010 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20149413     DOI: 10.1016/j.humpath.2009.10.019

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  23 in total

1.  Pancreas: Histological diagnostic criteria for autoimmune pancreatitis.

Authors:  Terumi Kamisawa; Tooru Shimosegawa
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2011-12-13       Impact factor: 46.802

Review 2.  Diagnostic evaluation of solid pancreatic masses.

Authors:  Jeffrey L Tokar; Rohit Walia
Journal:  Curr Gastroenterol Rep       Date:  2013-10

Review 3.  Clinical and pathophysiological issues associated with type 1 autoimmune pancreatitis.

Authors:  Kazushige Uchida; Hideaki Miyoshi; Tsukasa Ikeura; Masaaki Shimatani; Makoto Takaoka; Kazuichi Okazaki
Journal:  Clin J Gastroenterol       Date:  2016-02-10

Review 4.  Diagnosis and management of IgG4-related disease.

Authors:  Vinod S Hegade; Maria B Sheridan; Matthew T Huggett
Journal:  Frontline Gastroenterol       Date:  2018-10-31

5.  Cervical lymph nodes, thyroiditis and ophthalmopathy: the pleomorphic face of an immunoglobulin g4-related disease.

Authors:  Christophe Ghys; Michel Depierreux; Elçin Ozalp; Brigitte Velkeniers
Journal:  Eur Thyroid J       Date:  2014-11-29

6.  The similarity of Type 1 autoimmune pancreatitis to pancreatic ductal adenocarcinoma with significant IgG4-positive plasma cell infiltration.

Authors:  Yuri Fukui; Kazushige Uchida; Kimi Sumimoto; Takeo Kusuda; Hideaki Miyoshi; Masanori Koyabu; Tsukasa Ikeura; Yutaku Sakaguchi; Masaaki Shimatani; Toshiro Fukui; Mitsunobu Matsushita; Makoto Takaoka; Akiyoshi Nishio; Nobuaki Shikata; Noriko Sakaida; Yoshiko Uemura; Sohei Satoi; A-Hon Kwon; Kazuichi Okazaki
Journal:  J Gastroenterol       Date:  2012-10-05       Impact factor: 7.527

7.  Lymphoplasmacytic sclerosing pancreatitis without IgG4 tissue infiltration or serum IgG4 elevation: IgG4-related disease without IgG4.

Authors:  Phil A Hart; Thomas C Smyrk; Suresh T Chari
Journal:  Mod Pathol       Date:  2014-08-01       Impact factor: 7.842

8.  Comparison study of immunohistochemical staining for the diagnosis of type 1 autoimmune pancreatitis.

Authors:  Katsuyuki Miyabe; Kenji Notohara; Takahiro Nakazawa; Kazuki Hayashi; Itaru Naitoh; Shuya Shimizu; Hiromu Kondo; Michihiro Yoshida; Hiroaki Yamashita; Shuichiro Umemura; Yasuki Hori; Akihisa Kato; Satoru Takahashi; Hirotaka Ohara; Takashi Joh
Journal:  J Gastroenterol       Date:  2014-08-10       Impact factor: 7.527

9.  Combined membranous nephropathy and tubulointerstitial nephritis as a rare renal manifestation of IgG4-related disease: a case-based literature review.

Authors:  Wei Zhang; Jeffrey H Glaze; David Wynne
Journal:  CEN Case Rep       Date:  2018-02-01

10.  An initial exploration for comprehensive assessment of IgG4-related lung disease: analyses on the cases enrolled from a systematic review.

Authors:  An Wang; Jie Fan; Xiaofeng Chen; Shaohua Wang
Journal:  J Thorac Dis       Date:  2018-03       Impact factor: 2.895

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.